A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106398



Internal ID22015631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29553905..29553905hg38UCSC Ensembl
chr22:29949894..29949894hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106398
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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